Mucosal immunization with polymeric antigen BLSOmp31 using alternative delivery systems against Brucella ovis in rams.
Administration, Intranasal
/ veterinary
Administration, Ophthalmic
Animals
Bacterial Outer Membrane Proteins
/ immunology
Brucella Vaccine
/ administration & dosage
Brucella ovis
Brucellosis
/ prevention & control
Immunogenicity, Vaccine
Immunoglobulin A
/ blood
Interferon-gamma
/ metabolism
Male
Microspheres
Semen
/ microbiology
Sheep
Sheep Diseases
/ microbiology
Vaccines, Synthetic
/ immunology
BLSOmp31-Chitosan microspheres
BLSOmp31-Poloxamer 407-Chitosan gel
Brucella ovis
Immunogenicity
Lambs
Mucosal immunization
Partial protection
Journal
Veterinary immunology and immunopathology
ISSN: 1873-2534
Titre abrégé: Vet Immunol Immunopathol
Pays: Netherlands
ID NLM: 8002006
Informations de publication
Date de publication:
Mar 2019
Mar 2019
Historique:
received:
02
06
2018
revised:
05
02
2019
accepted:
09
02
2019
entrez:
20
3
2019
pubmed:
20
3
2019
medline:
27
3
2019
Statut:
ppublish
Résumé
Subcellular vaccines against ovine contagious epididymitis due Brucella ovis can solve some shortcomings associated with the use of Brucella melitensis Rev 1. We have demonstrated that the parenteral immunization with polymeric antigen BLSOmp31 emulsified in oil adjuvant conferred significant protection against B. ovis in rams. In our previous studies, we have characterized chitosan microspheres (ChMs) and a thermoresponsive and mucoadhesive in situ gel (Poloxamer 407-Ch) as two novel formulation strategies for the delivery of BLSOmp31 in nasal as well as conjunctival mucosa. In the present work, we evaluated the immunogenicity and protection conferred by the intranasal and conjunctival immunization with these two mucosal delivery systems against B. ovis in rams. BLSOmp31-ChM administered by intranasal route and BLSOmp31-P407-Ch applied by intranasal or conjunctival routes induced systemic, local and preputial IgG and IgA antibody response. Neither formulation showed interference in the serological diagnosis. Thus, mucosal immunization using either formulation induced significant specific cellular immune responses (in vitro and in vivo) and it prevented the excretion of B. ovis in semen. Although these vaccines did not prevent infection in immunized rams, colonization reduction of infected organs and bacterial distribution differed significantly between vaccinated and unvaccinated rams.
Identifiants
pubmed: 30885309
pii: S0165-2427(18)30237-X
doi: 10.1016/j.vetimm.2019.02.005
pii:
doi:
Substances chimiques
Bacterial Outer Membrane Proteins
0
Brucella Vaccine
0
Immunoglobulin A
0
Vaccines, Synthetic
0
Interferon-gamma
82115-62-6
Types de publication
Clinical Trial, Veterinary
Comparative Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
70-77Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.